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Seed amplification and neurodegeneration marker trajectories in individuals at risk of prion disease.
Mok TH, Nihat A, Majbour N, Sequeira D, Holm-Mercer L, Coysh T, Darwent L, Batchelor M, Groveman BR, Orr CD, Hughson AG, Heslegrave A, Laban R, Veleva E, Paterson RW, Keshavan A, Schott JM, Swift IJ, Heller C, Rohrer JD, Gerhard A, Butler C, Rowe JB, Masellis M, Chapman M, Lunn MP, Bieschke J, Jackson GS, Zetterberg H, Caughey B, Rudge P, Collinge J, Mead S. Mok TH, et al. Among authors: schott jm. Brain. 2023 Jun 1;146(6):2570-2583. doi: 10.1093/brain/awad101. Brain. 2023. PMID: 36975162 Free PMC article.
Cerebral microbleeds in familial Alzheimer's disease.
Ryan NS, Bastos-Leite AJ, Rohrer JD, Werring DJ, Fox NC, Rossor MN, Schott JM. Ryan NS, et al. Among authors: schott jm. Brain. 2012 Jan;135(Pt 1):e201; author reply e202. doi: 10.1093/brain/awr126. Epub 2011 Jun 17. Brain. 2012. PMID: 21685457 Free PMC article. No abstract available.
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration.
Rohrer JD, Lashley T, Schott JM, Warren JE, Mead S, Isaacs AM, Beck J, Hardy J, de Silva R, Warrington E, Troakes C, Al-Sarraj S, King A, Borroni B, Clarkson MJ, Ourselin S, Holton JL, Fox NC, Revesz T, Rossor MN, Warren JD. Rohrer JD, et al. Among authors: schott jm. Brain. 2011 Sep;134(Pt 9):2565-81. doi: 10.1093/brain/awr198. Brain. 2011. PMID: 21908872 Free PMC article.
Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.
Beck J, Poulter M, Hensman D, Rohrer JD, Mahoney CJ, Adamson G, Campbell T, Uphill J, Borg A, Fratta P, Orrell RW, Malaspina A, Rowe J, Brown J, Hodges J, Sidle K, Polke JM, Houlden H, Schott JM, Fox NC, Rossor MN, Tabrizi SJ, Isaacs AM, Hardy J, Warren JD, Collinge J, Mead S. Beck J, et al. Among authors: schott jm. Am J Hum Genet. 2013 Mar 7;92(3):345-53. doi: 10.1016/j.ajhg.2013.01.011. Epub 2013 Feb 21. Am J Hum Genet. 2013. PMID: 23434116 Free PMC article.
Molecular nexopathies: a new paradigm of neurodegenerative disease.
Warren JD, Rohrer JD, Schott JM, Fox NC, Hardy J, Rossor MN. Warren JD, et al. Among authors: schott jm. Trends Neurosci. 2013 Oct;36(10):561-9. doi: 10.1016/j.tins.2013.06.007. Epub 2013 Jul 19. Trends Neurosci. 2013. PMID: 23876425 Free PMC article.
Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia.
Rohrer JD, Beck J, Plagnol V, Gordon E, Lashley T, Revesz T, Janssen JC, Fox NC, Warren JD, Rossor MN, Mead S, Schott JM. Rohrer JD, et al. Among authors: schott jm. J Neurol Neurosurg Psychiatry. 2013 Dec;84(12):1411-2. doi: 10.1136/jnnp-2013-306116. Epub 2013 Jul 31. J Neurol Neurosurg Psychiatry. 2013. PMID: 23904625 Free PMC article. No abstract available.
364 results